No Arabic abstract
Electrons on liquid helium can form different phases depending on density, and temperature. Also the electron-ripplon coupling strength influences the phase diagram, through the formation of so-called ripplonic polarons, that change how electrons are localized, and that shifts the transition between the Wigner solid and the liquid phase. We use an all-coupling, finite-temperature variational method to study the formation of a ripplopolaron Wigner solid on a liquid helium film for different regimes of the electron-ripplon coupling strength. In addition to the three known phases of the ripplopolaron system (electron Wigner solid, polaron Wigner solid, and electron fluid), we define and identify a fourth distinct phase, the ripplopolaron liquid. We analyse the transitions between these four phases and calculate the corresponding phase diagrams. This reveals a reentrant melting of the electron solid as a function of temperature. The calculated regions of existence of the Wigner solid are in agreement with recent experimental data.
The second-layer phase diagrams of $^4$He and $^3$He adsorbed on graphite are investigated. Intrinsically rounded specific-heat anomalies are observed at 1.4 and 0.9 K, respectively, over extended density regions in between the liquid and incommensurate solid phases. They are identified to anomalies associated with the Kosterlitz-Thouless-Halperin-Nelson-Young type two-dimensional melting. The prospected low temperature phase (C2 phase) is a commensurate phase or a $textit{quantum hexatic}$ phase with quasi-bond-orientational order, both containing $textit{zero}$-$textit{point}$ defectons. In either case, this would be the first atomic realization of the $textit{quantum liquid crystal}$, a new state of matter. From the large enhancement of the melting temperature over $^3$He, we propose to assign the observed anomaly of $^4$He-C2 phase at 1.4 K to the hypothetical supersolid or superhexatic transition.
A concentration-saturated helium mixture at the melting pressure consists of two liquid phases and one or two solid phases. The equilibrium system is univariant, whose properties depend uniquely on temperature. Four coexisting phases can exist on singular points, which are called quadruple points. As a univariant system, the melting pressure could be used as a thermometric standard. It would provide some advantages compared to the current reference, namely pure $^3$He, especially at the lowest temperatures below 1 mK. We have extended the melting pressure measurements of the concentration-saturated helium mixture from 10 mK to 460 mK. The density of the dilute liquid phase was also recorded. The effect of the equilibrium crystal structure changing from hcp to bcc was clearly seen at T=294 mK at the melting pressure P=2.638 MPa. We observed the existence of metastable solid phases around this point. No evidence was found for the presence of another, disputed, quadruple point at around 400 mK. The experimental results agree well with our previous calculations at low temperatures, but deviate above 200 mK.
We present neutron scattering measurements of the dynamic structure factor, $S(Q,omega)$, of amorphous solid helium confined in 47 $AA$ pore diameter MCM-41 at pressure 48.6 bar. At low temperature, $T$ = 0.05 K, we observe $S(Q,omega)$ of the confined quantum amorphous solid plus the bulk polycrystalline solid between the MCM-41 powder grains. No liquid-like phonon-roton modes, other sharply defined modes at low energy ($omega<$ 1.0 meV) or modes unique to a quantum amorphous solid that might suggest superflow are observed. Rather the $S(Q,omega)$ of confined amorphous and bulk polycrystalline solid appear to be very similar. At higher temperature ($T>$ 1 K), the amorphous solid in the MCM-41 pores melts to a liquid which has a broad $S(Q,omega)$ peaked near $omega simeq$ 0 characteristic of normal liquid $^4$He under pressure. Expressions for the $S(Q,omega)$ of amorphous and polycrystalline solid helium are presented and compared. In previous measurements of liquid $^4$He confined in MCM-41 at lower pressure the intensity in the liquid roton mode decreases with increasing pressure until the roton vanishes at the solidification pressure (38 bars), consistent with no roton in the solid observed here.
The finite temperature phase diagram of two-dimensional dipolar bosons versus dipolar interaction strength is discussed. We identify the stable phases as dipolar superfluid (DSF), dipolar Wigner crystal (DWC), dipolar hexatic fluid (DHF), and dipolar normal fluid (DNF). We also show that other interesting phases like dipolar supersolid (DSS) and dipolar hexatic superfluid (DHSF) are at least metastable, and can potentially be reached by thermal quenching. In particular, for large densities or strong dipolar interactions, we find that the DWC exists at low temperatures, but melts into a DHF at higher temperatures, where translational crystaline order is destroyed but orientational order is preserved. Upon further increase in temperature the DHF phase melts into the DNF, where both orientational and translational lattice order are absent. Lastly, we discuss the static structure factor for some of the stable phases and show that they can be identified via optical Bragg scattering measurements.
A sufficiently large perpendicular magnetic field quenches the kinetic (Fermi) energy of an interacting two-dimensional (2D) system of fermions, making them susceptible to the formation of a Wigner solid (WS) phase in which the charged carriers organize themselves in a periodic array in order to minimize their Coulomb repulsion energy. In low-disorder 2D electron systems confined to modulation-doped GaAs heterostructures, signatures of a magnetic-field-induced WS appear at low temperatures and very small Landau level filling factors ($ usimeq1/5$). In dilute GaAs 2D textit{hole} systems, on the other hand, thanks to the larger hole effective mass and the ensuing Landau level mixing, the WS forms at relatively higher fillings ($ usimeq1/3$). Here we report our measurements of the fundamental temperature vs. filling phase diagram for the 2D holes WS-liquid textit{thermal melting}. Moreover, via changing the 2D hole density, we also probe their Landau level mixing vs. filling WS-liquid textit{quantum melting} phase diagram. We find our data to be in good agreement with the results of very recent calculations, although intriguing subtleties remain.